Canonical Allele Identifier: CA1821060319

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133029907G= , CM000670.2:g.133029907G=	GRCh38
NC_000008.10:g.134042152G= , CM000670.1:g.134042152G=	GRCh37
NC_000008.9:g.134111334G=	NCBI36
NG_015832.1:g.167948G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003235.5:c.7123G= MANE Select	NP_003226.4:p.Gly2375=
ENST00000220616.9:c.7123G= MANE Select	ENSP00000220616.4:p.Gly2375=
NM_003235.4:c.7123G=	NP_003226.4:p.Gly2375=
ENST00000220616.8:c.7123G=	ENSP00000220616.4:p.Gly2375=
ENST00000518108.1:c.509G=
ENST00000519178.5:c.2489G=
ENST00000519543.5:c.1522G=	ENSP00000430430.1:p.Gly508=
ENST00000523756.5:c.3778G=
XM_005251038.3:c.6931G=	XP_005251095.1:p.Gly2311=
XM_005251038.4:c.6931G=	XP_005251095.1:p.Gly2311=
XM_006716622.2:c.7060G=	XP_006716685.1:p.Gly2354=
XM_006716622.3:c.7060G=	XP_006716685.1:p.Gly2354=
XM_017013793.1:c.7057G=	XP_016869282.1:p.Gly2353=
XM_017013794.1:c.7123G=	XP_016869283.1:p.Gly2375=
XM_017013795.1:c.6952G=	XP_016869284.1:p.Gly2318=
XM_017013796.1:c.6904G=	XP_016869285.1:p.Gly2302=
XM_017013797.1:c.6862G=	XP_016869286.1:p.Gly2288=
XM_017013798.1:c.7123G=	XP_016869287.1:p.Gly2375=